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Chemical Structure| 62621-10-7 Chemical Structure| 62621-10-7

Structure of 62621-10-7

Chemical Structure| 62621-10-7

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Product Details of [ 62621-10-7 ]

CAS No. :62621-10-7
Formula : C10H11NO4
M.W : 209.20
SMILES Code : O=C(OCC)C1=CC=C([N+]([O-])=O)C=C1C
MDL No. :MFCD11111003

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Application In Synthesis of [ 62621-10-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 62621-10-7 ]

[ 62621-10-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 62621-10-7 ]
  • [ 74450-59-2 ]
YieldReaction ConditionsOperation in experiment
93.94% With hydrogen;nickel; In methanol; under 2585.81 Torr; for 2.0h; Compound of example la (41g; 196 mmol) in MeOH (500 ml) was hydrogenated using Raney Ni (2g) at 50 psi for 2h. The solution was filtered free off the catalyst, concentrated and purified using flash chromatography (silica gel, 10% EtOAc-PE 60-80C, 30% EtOAc-PE 60- 80C) to obtain the title compound. Yield, 33g (93.94%) ; mp, 77-80C, MS (EI) : 179 (M+), 134 (100%), 106,77 ; analysis: C10H13NO2 requires, C, 67.02 ; H, 7.31 ; N, 7.82 ; found, C, 67.25 ; H, 7.26 ; N, 7.57%.
93.94% With hydrogen;Raney Ni; In methanol; under 2585.81 Torr; for 2.0h; Example 1b 4-Amino-2-methyl-benzoic acid ethyl ester Compound of example 1a (41 g; 196 mmol) in MeOH (500 ml) was hydrogenated using Raney Ni (2 g) at 50 psi for 2 h. The solution was filtered free off the catalyst, concentrated and purified using flash chromatography (silica gel, 10% EtOAc-PE 60-80 C., 30% EtOAc-PE 60-80 C.) to obtain the title compound. Yield, 33 g (93.94%); mp, 77-80 C., MS (EI): 179 (M+), 134 (100%), 106, 77; analysis: C10H13NO2 requires, C, 67.02; H, 7.31; N, 7.82; found, C, 67.25; H, 7.26; N, 7.57%.
 

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